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Chronobiological analysis of circadian patterns in transcription of seven key clock genes in six peripheral tissues in mice

机译:小鼠六种周围组织中七个关键时钟基因转录的昼夜节律模式的时序生物学分析

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The molecular clock machinery in mammals consists of a number of clock genes (CGs) and their resultant proteins that form interlocking tran scription-translation feedback loops. These loops generate and maintain the 24 h mRNA and protein oscillations and consequential biological and physiological rhythms. To understand whether peripheral oscillators share similarly-timed clock machinery, the temporal expression patterns of the seven recognized key CGs (mPer1, mPer2, mCry1, mCry2, mRev-erb alpha, mClock, and raBmall) were examined simultaneously in six peripheral tissues in mice every 4 It for 24 h in synchronized light-dark conditions using real time PCR assays. Time series were analyzed for time-effect by ANOVA and for rhythm characteristics by the single cosinor fitting procedure. The expression levels of most CGs were comparable in liver, kidney, and spleen, but mBmall and mCry1 were more abundant in the thymus, and mPerl, mCry1, and mCry2 were more abundant in the testis. In addition, mCry2 was dramatically lower in the kidney, spleen, and thymus; mPer2 was significantly lower in the spleen, testis, and thymus; and all of the genes tested were strikingly less abundant in peripheral blood. A significant 24 h rhythmic component was found for each CG in the liver and kidney and for some CGs in other tissues. Of note, a 12 h ultradian rhythmic component was also found in mRNA expression for some CGs in several of the tissues and was the only significant oscillation observed for CGs in the testis. Ultradian oscillations were also observed for mPer1 in the testis (8 h) and thymus (12 h and 8 h) in a second study where mice were sampled every 2 h. The present results suggest that the functioning of the molecular circadian clock may be modified to some extent between peripheral tissues, as denoted by differences in amplitude and phasing, and operates differently or is less developed in tissues
机译:哺乳动物中的分子时钟机制由许多时钟基因(CG)及其形成的蛋白质组成,这些蛋白质形成互锁的转录-翻译反馈环。这些循环产生并维持24小时的mRNA和蛋白质振荡以及随之而来的生物学和生理节律。为了了解外围振荡器是否共享类似定时的时钟机制,在小鼠的六个外围组织中同时检查了七个公认的关键CG(mPer1,mPer2,mCry1,mCry2,mRev-erb alpha,mClock和raBmall)的时间表达模式。使用实时PCR分析法,在同步的明暗条件下每4小时进行24小时。通过ANOVA分析时间序列的时间效果,并通过单余弦拟合程序分析节奏特征。大多数CGs的表达水平在肝脏,肾脏和脾脏中相当,但在胸腺中mBmall和mCry1更为丰富,在睾丸中mPerl,mCry1和mCry2更为丰富。此外,肾脏,脾脏和胸腺中的mCry2含量显着降低。脾,睾丸和胸腺中的mPer2明显降低;而且所有测试的基因在外周血中的丰富程度都显着降低。在肝脏和肾脏中的每个CG以及其他组织中的某些CG中,发现了重要的24小时节律成分。值得注意的是,在一些组织中某些CG的mRNA表达中也发现了12小时的超节奏节律成分,这是睾丸中CG唯一观察到的明显振荡。在第二个研究中,每2小时对小鼠取样一次,在睾丸(8 h)和胸腺(12 h和8 h)中也观察到mPer1的超摆动。目前的结果表明,分子生物钟的功能可能会在周围组织之间进行一定程度的修改,如幅度和相位的差异所示,并且在组织中的运作方式不同或发展程度较低。

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